FDA label 428691a1-5357-4afa-a7a8-1e9f2b22e43b

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
0797ae5e-8b81-4ca5-8452-68578c4f8379
SPL ID
428691a1-5357-4afa-a7a8-1e9f2b22e43b
Version
1
Effective date
2019-05-21
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:20:07

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings When using this product avoid unnecessary sun exposure and use a sunscreen. ■ For external use only ■ Keep away from eyes, lips, and mouth ■ If irritation develops discontinue use and consult a doctor ■ Using other topical acne medications at the same time or immediately, following use of this product may increase dryness or irritation of the skin. If this occurs consult a doctor. ■May bleach fabrics.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.